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The QA Specialist conducts investigations and assists with related incident management tasks and documentation. The Quality Assurance Specialist is responsible for all aspects of internal incident management /trending and the tracking of RIA documentation to ensure compliance with regulation.
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Perform records review or pre-shipment review and file daily documentation (Red Zone, smart sheets, and lucid chard). Perform annual internal policy review and provide updates to QA System Coordinator for review.
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Position Summary: The QA Sr. Specialist will execute quality assurance related activities to ensure compliance with end to end operations (manufacturing, supply chain, QC, etc.) The position requires diverse skill sets and will provide the opportunity to challenge an individual's abilities to perform training, batch records review, data review to implement sound Quality System improvements, documentation review, deviation and CAPA management, change control, etc.
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The Change Control Plant QA Specialist may be responsible for daily technical support for change control and document control activities of the Documentation Technicians. The Change Control Plant QA Specialist may also be responsible for daily technical support for change control and document control activities of the Documentation Technicians.
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Join us as a QA Specialist, where you'll handle QA activities that directly support the execution of the process within the Process Execution Team (PET) and in assigned areas outside of the PETs. This includes batch release, change control and documentation, equipment and process validation, deviation investigations, SOPs, supplier management, distribution center management, and regulatory interactions.
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As a Medical QA Specialist, you will work closely with medical providers and the Veterans Administration to ensure the documentation process is complete and accurate. Leidos QTC Health Services is seeking a Medical Quality Assurance (QA) Specialist to support our Veteran Affairs Operations in Philadelphia, PA.
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Employment as a QA will include successful completion of a 120-day probationary period during which you will be given objectives to achieve. In this role, you will review documentation sent over from medical providers and ensure the report is complete, concise, clear, and correct and the provider has accurately completed the Disability Benefit Questionnaires for delivery back to the VA.
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The Reimbursement Quality Audit & Documentation Specialist will work closely with the Reimbursement QA Supervisor to perform quality assurance activities with the focus on monitoring and improving reimbursement collection efforts.
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Proclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company. QA Specialist - Contract - Onsite. Knowledge and expertise of quality systems in a pharmaceutical environment, such as, Deviation, Documentation Management, Training, Change Control, CAPA.
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The QA Documentation Specialist works directly with the QA Supervisor and QA Manager to ensure product safety and quality programs and systems are met for all products produced.
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The Sr. QA Specialist will be responsible for supporting QA processes, including, Vendor Management, Change Control, Training and Management Review. Previous experience working with quality systems having oversight of GxP operations including some or all of the following: Document Control, Training, Change Control, Management Review, Batch Documentation.
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Procures technical information from QA/QC databases for the NOW sales teams for regulatory and registration requests. For documentation and registration work, confirms accuracy and correctness of documentation from master formula to label listing of ingredients, content and claims, conformance to GMP and other regulatory requirements.
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The QA Specialist will support all activities related to testing, documentation, and investigations. Piper Companies is currently seeking a QA Specialist based in Fort Washington, Pennsylvania for work at a leading consumer testing company.
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Works closely with QC manager to communicate with Site Leadership and Velocity QA regarding any protocol deviations, good documentation practices deficiencies and any identified potential staff training requirements.
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Manage Pepperidge Farm QA documentation including creating new documents, revising existing documents, determining training needs, overseeing the approval and distribution processes, maintaining document control database and coordinating document reviews.
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